Evidence map›Paper›PMID 25574848›Full record

ArticleRedox biology2015

Annexin II-dependent actin remodelling evoked by hydrogen peroxide requires the metalloproteinase/sphingolipid pathway.

Christel Cinq-Frais, Christelle Coatrieux, Aude Savary, Romina D'Angelo, Corinne Bernis, Robert Salvayre, Anne Nègre-Salvayre, Nathalie Augé

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. FOXD1-dependent RalA-ANXA2-Src complex promotes CTC formation in breast cancer.Journal of experimental & clinical cancer research : CR · 2022
    Article
  6. Control of actin polymerizationFrontiers in cell and developmental biology · 2022
    Review
  7. Review
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Christel Cinq-FraisINSERM UMR-1048, Toulouse, France; Dept de Biochimie, CHU Rangueil, Toulouse, France; Université Paul Sabatier, Toulouse, France.
Christelle CoatrieuxINSERM UMR-1048, Toulouse, France; Dept de Biochimie, CHU Rangueil, Toulouse, France; Université Paul Sabatier, Toulouse, France.
Aude SavaryINSERM UMR-1048, Toulouse, France; Dept de Biochimie, CHU Rangueil, Toulouse, France; Université Paul Sabatier, Toulouse, France.
Romina D'AngeloINSERM UMR-1048, Toulouse, France.
Corinne BernisINSERM UMR-1048, Toulouse, France.
Robert SalvayreINSERM UMR-1048, Toulouse, France; Dept de Biochimie, CHU Rangueil, Toulouse, France; Université Paul Sabatier, Toulouse, France.
Anne Nègre-SalvayreINSERM UMR-1048, Toulouse, France; Université Paul Sabatier, Toulouse, France.
Nathalie AugéINSERM UMR-1048, Toulouse, France; Université Paul Sabatier, Toulouse, France. Electronic address: nathalie.auge@inserm.fr.
Hôpital Rangueil · FRInserm · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Actin remodeling is a dynamic process associated with cell shape modification occurring during cell cycle and proliferation. Oxidative stress plays a role in actin reorganization via various systems including p38MAPK. Beside, the mitogenic response evoked by hydrogen peroxide (H2O2) in fibroblasts and smooth muscle cells (SMC) involves the metalloproteinase (MMPs)/sphingomyelinase 2 (nSMase2) signaling pathway. The aim of this work was to investigate whether this system plays a role in actin remodeling induced by H2O2. Low H2O2 dose (5µM) rapidly triggered a signaling cascade leading to nSMase2 activation, src and annexin 2 (AnxA2) phosphorylation, and actin remodeling, in fibroblasts and SMC. These events were blocked by pharmacological inhibitors of MMPs (Ro28-2653) and p38MAPK (SB203580), and were lacking in MMP2(-/-) and in nSMase2-mutant (fro) fibroblasts. Likewise, H2O2 was unable to induce actin remodeling in fro and MMP2(-/-) fibroblasts or in cells pretreated with p38MAPK, or MMP inhibitors. Finally we show that nSMase2 activation by H2O2, depends on MMP2 and p38MAPK, and is required for the src-dependent phosphorylation of AnxA2, and actin remodeling. Taken together, these findings indicate for the first time that AnxA2 phosphorylation and actin remodeling evoked by oxidative stress depend on the sphingolipid pathway, via MMP2 and p38MAPK.

Indexed as

ActinsAnimalsAnnexin A2Cell ProliferationFibroblastsHumansHydrogen PeroxideMatrix Metalloproteinase 2MiceMyocytes, Smooth MuscleOxidative Stressp38 Mitogen-Activated Protein KinasesPhosphorylationSignal TransductionSphingolipidsActinsAnnexin A2Hydrogen PeroxideMatrix Metalloproteinase 2MMP2 protein, humanp38 Mitogen-Activated Protein KinasesSphingolipidsActinFibroblastsOxidative stressSmooth muscle cellsSphingolipidsVasculo-proliferative diseases

Identifiers

PMID25574848
PMCPMC4309845
OpenAlexW2091857182

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.